This variation has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/A/G/T | Ancestral: C | Ambiguity code: N
Location

Chromosome 3:41224610 (forward strand) | View in location tab

Co-located

with COSMIC COSM5677 (C/G), COSM5669 (C/T), COSM5673 (C/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 9 synonyms - click the plus to show

This variation has 60 HGVS names - click the plus to show

Variation displays